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Open a scheduled administration and verify that the patient, order, and intended record match.
Nuclear Medicine Workflow Software
In Development · Functional Synthetic PrototypeNuclide Dose Hub is a documentation, delivery, and reconciliation concept for nuclear medicine departments. It brings the scheduled order, dose administration record, final review, delivery status, exceptions, and audit history into one controlled workspace.
The Problem
A technologist may enter the same patient, radiopharmaceutical, assay, residual, administration, and sign-off details into several systems without a single view showing whether every destination accepted the information.
Product Goal
Verify the patient and order, document the administration, review and attest it, send approved data through authorized interfaces, and keep exceptions visible until they are resolved.
Proposed Workflow
The current prototype demonstrates this sequence with fictional patients, synthetic dose values, and clearly simulated destination systems.
Open a scheduled administration and verify that the patient, order, and intended record match.
Capture radiopharmaceutical, assay, residual, route, site, times, identifiers, and notes once.
Validate required fields, chronology, calculations, and consistency before final attestation.
Track acknowledgments and keep missing, mismatched, or failed records visible until resolved.
Current Prototype
These are working behaviors in the synthetic prototype, not claims of hospital integration or clinical validation.
Organize synthetic scheduled administrations by due, complete, and needs-attention status.
Keep patient and order verification, dose details, administration information, and notes together.
Check required fields, chronology, residual versus assay, and calculated net administered activity.
Summarize the record and require an explicit technologist attestation before simulated delivery.
Show labeled demonstration acknowledgments for EHR, RIS, PACS, and radiation-safety destinations.
Retry or resolve synthetic exceptions, review activity history, and export a demonstration CSV.
Future Integration
Source systems, required destinations, vendors, interfaces, and responsibility for each value would be identified during an authorized workflow review before any production design.
Prototype Boundary
The demonstration is not connected to a hospital, dose calibrator, scanner, EHR, RIS, PACS, or regulatory system. It is not a treatment-planning tool, clinical decision system, validated medical device, or replacement for hospital policy. No AI is used in the documentation, calculation, validation, delivery, acknowledgment, or reconciliation path.
All displayed patients, values, destinations, receipts, and audit events are fictional or simulated. Production use would require a hospital sponsor, supported vendor interfaces, security and privacy review, clinical validation, regulatory review, training, and formal acceptance.
Guided Synthetic Demonstration
A useful review identifies the real systems touched, repeated fields, source of truth for each value, exception cases, and who signs, corrects, or audits the record.
Do not send patient information, clinical screenshots, credentials, internal addresses, security details, policies, or confidential hospital material with an inquiry.